159 related articles for article (PubMed ID: 16221676)
1. G betagamma binds histone deacetylase 5 (HDAC5) and inhibits its transcriptional co-repression activity.
Spiegelberg BD; Hamm HE
J Biol Chem; 2005 Dec; 280(50):41769-76. PubMed ID: 16221676
[TBL] [Abstract][Full Text] [Related]
2. Loss of association between activated Galpha q and Gbetagamma disrupts receptor-dependent and receptor-independent signaling.
Evanko DS; Thiyagarajan MM; Takida S; Wedegaertner PB
Cell Signal; 2005 Oct; 17(10):1218-28. PubMed ID: 16038796
[TBL] [Abstract][Full Text] [Related]
3. mHDA1/HDAC5 histone deacetylase interacts with and represses MEF2A transcriptional activity.
Lemercier C; Verdel A; Galloo B; Curtet S; Brocard MP; Khochbin S
J Biol Chem; 2000 May; 275(20):15594-9. PubMed ID: 10748098
[TBL] [Abstract][Full Text] [Related]
4. Class II histone deacetylases are directly recruited by BCL6 transcriptional repressor.
Lemercier C; Brocard MP; Puvion-Dutilleul F; Kao HY; Albagli O; Khochbin S
J Biol Chem; 2002 Jun; 277(24):22045-52. PubMed ID: 11929873
[TBL] [Abstract][Full Text] [Related]
5. Regulation of G-protein signaling by RKTG via sequestration of the G betagamma subunit to the Golgi apparatus.
Jiang Y; Xie X; Zhang Y; Luo X; Wang X; Fan F; Zheng D; Wang Z; Chen Y
Mol Cell Biol; 2010 Jan; 30(1):78-90. PubMed ID: 19884349
[TBL] [Abstract][Full Text] [Related]
6. Identification of the ankyrin repeat proteins ANKRA and RFXANK as novel partners of class IIa histone deacetylases.
Wang AH; Grégoire S; Zika E; Xiao L; Li CS; Li H; Wright KL; Ting JP; Yang XJ
J Biol Chem; 2005 Aug; 280(32):29117-27. PubMed ID: 15964851
[TBL] [Abstract][Full Text] [Related]
7. RACK1 binds to a signal transfer region of G betagamma and inhibits phospholipase C beta2 activation.
Chen S; Lin F; Hamm HE
J Biol Chem; 2005 Sep; 280(39):33445-52. PubMed ID: 16051595
[TBL] [Abstract][Full Text] [Related]
8. Neuronal activity-dependent nucleocytoplasmic shuttling of HDAC4 and HDAC5.
Chawla S; Vanhoutte P; Arnold FJ; Huang CL; Bading H
J Neurochem; 2003 Apr; 85(1):151-9. PubMed ID: 12641737
[TBL] [Abstract][Full Text] [Related]
9. Histone deacetylase 5 acquires calcium/calmodulin-dependent kinase II responsiveness by oligomerization with histone deacetylase 4.
Backs J; Backs T; Bezprozvannaya S; McKinsey TA; Olson EN
Mol Cell Biol; 2008 May; 28(10):3437-45. PubMed ID: 18332106
[TBL] [Abstract][Full Text] [Related]
10. A2A adenosine-receptor-mediated facilitation of noradrenaline release in rat tail artery involves protein kinase C activation and betagamma subunits formed after alpha2-adrenoceptor activation.
Fresco P; Oliveira JM; Kunc F; Soares AS; Rocha-Pereira C; Gonçalves J; Diniz C
Neurochem Int; 2007 Jul; 51(1):47-56. PubMed ID: 17493708
[TBL] [Abstract][Full Text] [Related]
11. A docking site for G protein βγ subunits on the parathyroid hormone 1 receptor supports signaling through multiple pathways.
Mahon MJ; Bonacci TM; Divieti P; Smrcka AV
Mol Endocrinol; 2006 Jan; 20(1):136-46. PubMed ID: 16099817
[TBL] [Abstract][Full Text] [Related]
12. SMRTE inhibits MEF2C transcriptional activation by targeting HDAC4 and 5 to nuclear domains.
Wu X; Li H; Park EJ; Chen JD
J Biol Chem; 2001 Jun; 276(26):24177-85. PubMed ID: 11304536
[TBL] [Abstract][Full Text] [Related]
13. betaL-betaM loop in the C-terminal domain of G protein-activated inwardly rectifying K(+) channels is important for G(betagamma) subunit activation.
Finley M; Arrabit C; Fowler C; Suen KF; Slesinger PA
J Physiol; 2004 Mar; 555(Pt 3):643-57. PubMed ID: 14724209
[TBL] [Abstract][Full Text] [Related]
14. RACK1 regulates directional cell migration by acting on G betagamma at the interface with its effectors PLC beta and PI3K gamma.
Chen S; Lin F; Shin ME; Wang F; Shen L; Hamm HE
Mol Biol Cell; 2008 Sep; 19(9):3909-22. PubMed ID: 18596232
[TBL] [Abstract][Full Text] [Related]
15. Involvement of the βγ subunits of G proteins in the cAMP response induced by stimulation of the histamine H1 receptor.
Maruko T; Nakahara T; Sakamoto K; Saito M; Sugimoto N; Takuwa Y; Ishii K
Naunyn Schmiedebergs Arch Pharmacol; 2005 Aug; 372(2):153-9. PubMed ID: 16189696
[TBL] [Abstract][Full Text] [Related]
16. SMRT-mediated co-shuttling enables export of class IIa HDACs independent of their CaM kinase phosphorylation sites.
Soriano FX; Chawla S; Skehel P; Hardingham GE
J Neurochem; 2013 Jan; 124(1):26-35. PubMed ID: 23083128
[TBL] [Abstract][Full Text] [Related]
17. Transcriptional regulation by the repressor of estrogen receptor activity via recruitment of histone deacetylases.
Kurtev V; Margueron R; Kroboth K; Ogris E; Cavailles V; Seiser C
J Biol Chem; 2004 Jun; 279(23):24834-43. PubMed ID: 15140878
[TBL] [Abstract][Full Text] [Related]
18. Constitutive signaling of the human cytomegalovirus-encoded receptor UL33 differs from that of its rat cytomegalovirus homolog R33 by promiscuous activation of G proteins of the Gq, Gi, and Gs classes.
Casarosa P; Gruijthuijsen YK; Michel D; Beisser PS; Holl J; Fitzsimons CP; Verzijl D; Bruggeman CA; Mertens T; Leurs R; Vink C; Smit MJ
J Biol Chem; 2003 Dec; 278(50):50010-23. PubMed ID: 14522997
[TBL] [Abstract][Full Text] [Related]
19. Molecular mechanism of transcriptional repression of AhR repressor involving ANKRA2, HDAC4, and HDAC5.
Oshima M; Mimura J; Yamamoto M; Fujii-Kuriyama Y
Biochem Biophys Res Commun; 2007 Dec; 364(2):276-82. PubMed ID: 17949687
[TBL] [Abstract][Full Text] [Related]
20. The DnaJ-related factor Mrj interacts with nuclear factor of activated T cells c3 and mediates transcriptional repression through class II histone deacetylase recruitment.
Dai YS; Xu J; Molkentin JD
Mol Cell Biol; 2005 Nov; 25(22):9936-48. PubMed ID: 16260608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]